Literature DB >> 22285282

It is "too late" or is it? Bereaved family member perceptions of hospice referral when their family member was on hospice for seven days or less.

Joan M Teno1, David Casarett, Carol Spence, Stephen Connor.   

Abstract

CONTEXT: Many family members of patients enrolled in hospice for less than seven days state that the hospice referral was made "at the right time."
OBJECTIVES: To examine bereaved family members' perceptions of the timing of hospice referral to identify aspects of the referral process that can be improved.
METHODS: Open-ended interviews were conducted in seven hospice programs, interviewing bereaved family members of hospice patients who died within the first week of hospice enrollment.
RESULTS: Of the 100 narrative interviews, 99 respondents stated that their family member was either referred "too late" (n=41) or "at the right time" (n=58) to hospice services. When families stated that referral was "at the right time," their perceptions were based on the patient having refused earlier referral (n=8), a rapid decline in the patient's condition resulting in the late referral (n=20), or a belief in all things coming together as they were meant to (n=11). In contrast, when families stated that referral was "too late," their reasons were centered on concerns with the health care providers' role in decision making (n=24), with the leading concerns being inadequate physician communication (n=7), not recognizing the patient as dying (n=11), or problematic hospice delays in referral from the nursing home or home health agency (n=4). Despite the patient refusing an earlier hospice referral, five family members believed the referral was "too late."
CONCLUSION: Whereas family members identified expected concerns with communication, more than one in three stated an earlier hospice referral was not possible.
Copyright © 2012 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22285282     DOI: 10.1016/j.jpainsymman.2011.05.012

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  23 in total

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Authors:  Amy Sexauer; M Jennifer Cheng; Louise Knight; Anthony W Riley; Lauren King; Thomas J Smith
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2.  The Developmental Transition From Living With to Dying From Cancer: Hospice Decision Making.

Authors:  Deborah Waldrop; Mary Ann Meeker; Jean S Kutner
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3.  Is Care for the Dying Improving in the United States?

Authors:  Joan M Teno; Vicki A Freedman; Judith D Kasper; Pedro Gozalo; Vincent Mor
Journal:  J Palliat Med       Date:  2015-04-29       Impact factor: 2.947

4.  Association Between Hospice Use and Depressive Symptoms in Surviving Spouses.

Authors:  Katherine A Ornstein; Melissa D Aldridge; Melissa M Garrido; Rebecca Gorges; Diane E Meier; Amy S Kelley
Journal:  JAMA Intern Med       Date:  2015-07       Impact factor: 21.873

5.  Ethics of a therapeutic trial: addressing limitations of an active intervention in optic nerve lymphoma.

Authors:  Rohan Bir Singh; Sahil Thakur; Parul Ichhpujani; Suresh Kumar
Journal:  BMJ Case Rep       Date:  2018-03-28

6.  Is It the Difference a Day Makes? Bereaved Caregivers' Perceptions of Short Hospice Enrollment.

Authors:  Deborah P Waldrop; Mary Ann Meeker; Jean S Kutner
Journal:  J Pain Symptom Manage       Date:  2016-05-24       Impact factor: 3.612

7.  Perceived timeliness of referral to hospice palliative care among bereaved family members in Korea.

Authors:  Hyun Jung Jho; Yoon Jung Chang; Hye Young Song; Jin Young Choi; Yeol Kim; Eun Jung Park; Soo Jin Paek; Hee Jae Choi
Journal:  Support Care Cancer       Date:  2015-03-05       Impact factor: 3.603

8.  Family Members' Experience With Hospice in Nursing Homes.

Authors:  L Ashley Gage; Karla Washington; Debra Parker Oliver; Robin Kruse; Alexandra Lewis; George Demiris
Journal:  Am J Hosp Palliat Care       Date:  2014-11-23       Impact factor: 2.500

9.  Qualitative Study of Patients' and Caregivers' Perceptions and Information Preferences About Hospice.

Authors:  Areej El-Jawahri; Lara Traeger; Jennifer A Shin; Helen Knight; Kristina Mirabeau-Beale; Joel Fishbein; Harry H Vandusen; Vicki A Jackson; Angelo E Volandes; Jennifer S Temel
Journal:  J Palliat Med       Date:  2017-05-30       Impact factor: 2.947

10.  Change in end-of-life care for Medicare beneficiaries: site of death, place of care, and health care transitions in 2000, 2005, and 2009.

Authors:  Joan M Teno; Pedro L Gozalo; Julie P W Bynum; Natalie E Leland; Susan C Miller; Nancy E Morden; Thomas Scupp; David C Goodman; Vincent Mor
Journal:  JAMA       Date:  2013-02-06       Impact factor: 56.272

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